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Hurles, Matthew E

TitleYearPMID
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. 2013 23563609
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants. 2011 21552272
Large, rare chromosomal deletions associated with severe early-onset obesity. 2010 19966786
Origins and functional impact of copy number variation in the human genome. 2010 19812545
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